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9 quires the successful interpretation of both phonetic and syllabic information in the auditory signal
12 change of phoneme at a native and nonnative phonetic boundary in full-term and preterm human infants
14 supramarginal gyrus: stimuli from different phonetic categories, when presented together in a contra
17 tributions, contextual theories propose that phonetic category learning is informed by higher-level p
18 r hyperarticulation of vowels elicits larger phonetic change responses, as indexed by the mismatch ne
20 language processes characterized by regular phonetic changes, that is, gradual changes in vowel pron
29 ics surveyed include categorical perception, phonetic context effects, learning of speech and related
31 an subjects with paired speech sounds from a phonetic continuum but diverted their attention from pho
35 ts the conclusion that early experience with phonetic contrasts of a language results in changes in n
36 s a variety of acoustic cues to auditory and phonetic contrasts that are exploited by the listener in
39 e roles of "association" and "simulation" in phonetic decoding, demonstrating that these two routes c
42 ic motor circuits are recruited that reflect phonetic distinctive features of the speech sounds encou
45 provide evidence that visual speech modifies phonetic encoding at the auditory cortex.SIGNIFICANCE ST
48 tionary solution corresponding to a state of phonetic equilibrium, in which speakers of all ages shar
49 ariables predicted speech identification and phonetic feature reception at both positive and negative
50 of the input, which operate in both acoustic-phonetic feature-based and articulatory-gestural domains
52 l cortex responded selectively to individual phonetic features defined on the basis of machine-extrac
57 mplicated in the invariant representation of phonetic forms and that this area also responds preferen
59 lterations that change the vowel's perceived phonetic identity; moreover, the effect generalizes acro
60 apid and effortless extraction of meaningful phonetic information from a highly variable acoustic sig
61 ime, one subfield has examined perception of phonetic information independent of its contribution to
63 temporal sulcus responds to the presence of phonetic information, but its anterior part only respond
65 en-language task, online accrual of acoustic-phonetic input and competition between partially active
66 ysis of the relationship between audiovisual phonetic input in comparison with stored knowledge, as h
69 Between 9 and 10 mo of age, infants show phonetic learning from live, but not prerecorded, exposu
70 The neural signatures of learning at the phonetic level can be documented at a remarkably early p
71 direct evidence for acoustic-to-higher order phonetic level encoding of speech sounds in human langua
72 t missing speech is restored at the acoustic-phonetic level in bilateral auditory cortex, in real-tim
78 cortex that allow for more robust automatic, phonetic processing of native-language speech input.
79 It has been suggested by Poeppel (2003) that phonetic processing requires an optimal time scale of 25
81 ld has been less concerned with the acoustic-phonetic properties of speech and more concerned with ho
82 he non-arbitrary mappings that exist between phonetic properties of speech sounds and their meaning.
83 life, infants acquire information about the phonetic properties of their native language simply by l
85 the split fovea assumption, the semantic and phonetic radicals are initially projected to and process
89 etic encoding by dynamically weighting which phonetic representation in the auditory cortex is streng
91 illusion, we show that visual context primes phonetic representations at the auditory cortex, alterin
95 obe neural selectivity, we observed acoustic-phonetic selectivity in left anterior and left posterior
96 mporal sulcus being to transiently represent phonetic sequences, whether heard or internally generate
97 at this area also responds preferentially to phonetic sounds, above artificial control sounds or envi
99 nt from infants' earliest brain responses to phonetic stimuli is reflected in their language and prer
103 ference may have existed before the onset of phonetic training, and that its presence confers an adva
105 x than nonexpert controls, and the amount of phonetic transcription training did not predict auditory
106 e size of left pars opercularis and years of phonetic transcription training experience, illustrating
108 capable of discerning differences among the phonetic units of all languages, including native- and f
110 There is evidence that early mastery of the phonetic units of language requires learning in a social
112 n in response adaptation to sound pairs with phonetic vs. spatial sound changes, demonstrating that t
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